This test is intended to be used as an aid to the diagnosis of bacterial vaginosis (BV) in women with a clinical presentation consistent with this disorder. Used to detect the presence of Candida albicans and Candida glabrata DNA in vaginal samples as an aid to the diagnosis of vulvovaginal candidiasis in symptomatic women. Also used in the diagnosis of Neisseria gonorrhoeae, and Trichomonas vaginalis infections.
Specimen Type
Swab
Container
Aptima Swab
Collection Instructions
Container/Tube: Aptima® Multitest Transport swab (Orange label) or Aptima® Unisex swab (White label) Specimen: One Aptima® Swab
Collection: Vaginal swab: Collect vaginal fluid sample using the Gen-Probe® Aptima® swab by contacting the swab Causes for Rejection Incorrect patient identification; unlabeled specimen; inappropriate specimen transport conditions, including specimens received frozen; specimen leaked in transit; specimen in expired transport or incorrect transport device; specimens with inappropriate source for test requested; specimen with fixative or additives; Aptima® urine transport; Aptima® swab transport >30 days from collection; Aptima® swab specimen without a swab; cleaning swab (white-shaft swab) in Aptima® swab transport; any non-Aptima® swab submitted in Aptima® transport device; transport device with multiple swabs; bloody or grossly mucoid specimens; bacterial swabs; specimen in ProbeTec™ UPT transport; ProbeTec™ Q-swabs to the lower third of the vaginal wall and rotating the swab for 10 to 30 seconds to absorb fluid. Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. Tightly screw on the cap.
Transport Instructions
Room Temperature
Specimen Stability
30 Days Room Temperature and Refrigerated Not Acceptable Frozen
Methodology
Nucleic acid amplification (NAA) Includes Candida albicans, Candida glabrata, Trichomonas vaginalis, Bacterial Vaginosis, Megaspheara species, Atopobium vaginalis, Mycoplasma hominis, Mycoplasma genitalium and Ureaplasma species
